EP0949356B1 - Oberflächenbehandeltes Metallkomponent für die Verstärkung von Strukturen für Produkte aus vulkanisiertem elastomerem Material und daraus hergestellter Gegenstand - Google Patents

Oberflächenbehandeltes Metallkomponent für die Verstärkung von Strukturen für Produkte aus vulkanisiertem elastomerem Material und daraus hergestellter Gegenstand Download PDF

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EP0949356B1
EP0949356B1 EP99200870A EP99200870A EP0949356B1 EP 0949356 B1 EP0949356 B1 EP 0949356B1 EP 99200870 A EP99200870 A EP 99200870A EP 99200870 A EP99200870 A EP 99200870A EP 0949356 B1 EP0949356 B1 EP 0949356B1
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alloy
weight
content
article
cobalt
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French (fr)
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EP0949356A1 (de
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Federico Pavan
Giuseppina Ratti
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Pirelli and C SpA
Pirelli Tyre SpA
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Pirelli Pneumatici SpA
Pirelli SpA
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    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00—Electroplating: Baths therefor
    • C25D3/02—Electroplating: Baths therefor from solutions
    • C25D3/56—Electroplating: Baths therefor from solutions of alloys
    • C25D3/565—Electroplating: Baths therefor from solutions of alloys containing more than 50% by weight of zinc
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C18/00—Alloys based on zinc
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/55—Boron-containing compounds
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2/00—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor
    • C23C2/04—Hot-dipping or immersion processes for applying the coating material in the molten state without affecting the shape; Apparatus therefor characterised by the coating material
    • C23C2/06—Zinc or cadmium or alloys based thereon
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/02—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings only including layers of metallic material
    • C23C28/021—Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D only coatings only including layers of metallic material including at least one metal alloy layer

Definitions

  • the present invention relates to a reinforcing structure for manufactured products made of vulcanized elastomeric material, which is surface-coated with a metal alloy and an article of manufacture comprising at least one metal wire surface-coated with a metal alloy and buried in a vulcanized elastomeric material.
  • the present invention relates to a reinforcing structure for manufactured products made of elastomeric material, which is surface-coated with a ZnMoX alloy where X is a metal chosen from the group comprising cobalt, iron and nickel.
  • the metal of choice for the said structure is steel.
  • its chemical properties are not excellent since they do not ensure good adhesion to the vulcanized elastomeric material and they impart poor corrosion resistance.
  • the coating should not interfere with the drawing process or cause any appreciable deterioration to the wire.
  • An alloy which has been used for a long time for coating steel wires for reinforcing manufactured products made of vulcanized elastomeric material is brass (copper/zinc alloy with about 70% copper (Cu) and 30% zinc).
  • the adhesion is promoted thanks to the formation of a thin layer of copper sulphide Cu x S by the sulphur itself or by known derivatives thereof present in the mixture as vulcanizing agents.
  • Said brass/elastomer adhesion failure may be partially opposed by adding some cobalt in the form of a salt (US 5 356 711). It is believed that cobalt reduces the electrical conductivity of the layer of copper sulphide; this would slow the diffusion rate of Zn ++ ions and, as a consequence, reduce the growing rate of the ZnO/Zn(OH) 2 interface layer which is responsible for the destruction of the Cu x S film and thus for the adhesion.
  • the resulting octonate steel suffers the drawbacks characteristically associated with copper, i.e. rapid degradation both of the adhesion to the vulcanized elastomeric material and of the corrosion protection.
  • French Patent FR 2,413,228 and FR 2,426,562 disclose a metal wire coated with a ternary alloy composed of brass and cobalt, with a cobalt content of betwen 0.5 and 30% by weight.
  • Appliction EP-A-0,694,631 describes a metal wire coated with a binary alloy composed of zinc and manganese, with a manganese content of between 5 and 80% by weight.
  • Application EP-A-0,669,409 describes a metal wire coated with a binary alloy composed of zinc and cobalt, with a cobalt content of less than 1% by weight.
  • a ZnMoX ternary alloy has a drawability, a corrosion-resistance and an adhesion to the vulcanized elastomeric material after age-hardening which are better than those afforded by brass, zinc alone or the Zn/Mn and Zn/Co binary alloys described in European patent applications Nos EP 694,631 and EP 669,409.
  • the present invention thus relates to a reinforcing structure for manufactured products made of vulcanized elastomeric material according to claim 1.
  • the molybdenum content in the alloy of the present invention is preferably of from 0.05 to 3% by weight, even more preferably of from 0.1 to 1% by weight.
  • the zinc content in the alloy of the present invention is preferably of from 95 to 99.9% by weight, even more preferably of from 98 to 99.5% by weight.
  • the content of the third metal is preferably of from 0.05 to 2% by weight, even more preferably of from 0.1 to 1% by weight.
  • the said surface coating layer is formed by electrodeposition on the surface of the said steel wire.
  • the thickness of the said coating layer on the steel wire, before drawing, is preferably of from 1 to 4 microns. However, after drawing, this thickness is typically of from 0.1 to 0.4 micron.
  • Preferred examples of zinc salts which are suitable for carrying out the electrodeposition process according to the invention are those chosen from the group comprising sulphate, sulphamate, hypophosphite, picrate, selenate and thiocyanate. Even more preferably, these are sulphate and sulphamate.
  • molybdenum salts which are suitable for carrying out the electrodeposition process according to the invention are those chosen from the group comprising tetrabromide, oxydibromide, oxytetrachloride, oxydichloride, oxypentachloride, oxytetrafluoride, metaphosphate, phosphide and ammoniacal complexes.
  • the molybdenum salt is the ammoniacal complex of empirical formula (NH 4 ) 6 Mo 7 O 24 .4H 2 O.
  • cobalt salts which are suitable for carrying out the electrodeposition process according to the invention are those chosen from the group comprising divalent cobalt iodate, fluorides or chlorides and divalent cobalt thiocyanate and sulphates. Even more preferably, the cobalt salt is divalent cobalt sulphate.
  • the electrolytic deposition of an alloy ZnMoX, in which X is a metal chosen from the group comprising cobalt, iron and nickel, onto a steel wire comprises passing the said steel wire through an electrolytic bath consisting of an aqueous solution of a zinc salt, a molybdenum salt and a salt of a metal X, the said electrolytic bath having:
  • the throughput speed of the said wire is of from 10 to 70 m/min, and even more typically of from 20 to 50 m/min.
  • the zinc salt is a sulphate. Even more typically, the zinc sulphate is zinc sulphate heptahydrate.
  • the molybdenum salt is an ammoniacal complex. Even more typically, it is the ammoniacal molybdenum complex (NH 4 ) 6 Mo 7 O 24 .4H 2 O.
  • the steel wire is immersed in an electrolytic bath comprising a molybdenum salt, a zinc salt and a cobalt salt.
  • the electrolytic bath of the embodiment has a temperature of from 20 to 40°C, a pH of from 2 to 4 and a cathode density of from 10 to 40 A/dm 2 .
  • the present invention relates to a manufactured product made of vulcanized elastomeric material according to claim 9.
  • said article is a tire, a conveyor belt, a trasmission belt or a flexilble hose.
  • a steel wire surface-coated with a ZnMoX alloy of the present invention has a better adhesion to the vulcanized elastomeric matrix than a steel wire coated with brass when said vulcanized elastomeric matrix comprises a suitable adhesion promoter corresponding to at least 0.2% by weight of bivalent cobalt metal with respect to the weight of the elastomeric material.
  • this invention provides an article of manufacture comprising at least one metal wire buried in a vulcanized elastomeric matrix according to claim 17.
  • the amount of said salt of bivalent cobalt corresponds to an amount of bivalent cobalt metal of from 0.2 to 1% by weight with respect to the weight of said elastomer.
  • said salt of bivalent cobalt is selected from the group comprising carboxylate compounds of formula (I) (R-CO-O) 2 Co wherein R is a C 6-24 aliphatic or aromatic group, cobalt-boron complexes of formula (II) wherein R', R" and R"', equal or different each other, are a C 6-24 aliphatic or aromatic group, and mixture thereof.
  • R-CO-O-, R'-CO-O-, R"-CO-O- and R"'-CO-O- are those selected from the group comprising n-heptanoate, 2,2-dimethyl pentanoate, 2-ethyl-pentanotate, 4,4-dimethyl-pentanoate, 2-ethyl-esanoate, n-octanoate, 2,2-dimethyl-esanoate, neodecanoate and naphthenate.
  • a preferred example of a salt of formula (I) is cobalt neodecanoate.
  • a preferred example of a salt of formula (II) is cobalt-boron 2-ethyl-esanoate-neodecanoate.
  • the mixture may further comprise other conventional ingredients such as, for example, silica, resorcin and hexamethoxymethylamine.
  • Figure 2 shows a tire made of a vulcanized elastomeric matrix and a reinforcing structure comprising at least one steel wire coated with a layer of a ZnMoX alloy as above defined.
  • the vulcanized elastomeric matrix of said tire is obtained from a mixture comprising at least one vulcanizible elastomer, at least one vulcanizing agent consisting of sulphur or a derivative thereof, and a salt of bivalent cobalt selected from the group comprising cobalt-boron 2-ethyl-esanoate-neodecanoate and cobalt neodecanoate according to the present invention.
  • Said tire is mounted on a rim 13, and is composed of: bead 10, bead core 12, carcass ply 14, belt 15, tread 16 and sidewalls 17.
  • the belts 15 are made of cords of steel wire coated with a layer of a ZnMoX alloy as above defined.
  • Figures 3 through 5 show a conveyor belt 20, a transmission belt 30 and a flexible hose 40, respectively, each of which is made of a vulcanized elastomeric matrix reinforced by cords 15 made of steel wires coated with a layer of ZnMoX alloy as above defined.
  • the vulcanized elastomeric matrix is obtained from a mixture comprising at least one vulcanizible elastomer, at least one vulcanizing agent consisting of sulphur or a derivative thereof, and a salt of bivalent cobalt selected from the group comprising cobalt-boron 2-ethyl-esanoate-neodecanoate and cobalt neodecanoate according to the present invention.
  • 3x4x0.22 means a cord made of 3 strands, each of them made of 4 wires of 0.22 mm in diameter.
  • the amounts of the components of the vulcanizable mixtures exemplified are expressed in parts by weight.
  • a galvanic bath capable of depositing on a steel wire a layer of a zinc/cobalt/molybdenum ternary alloy consisting of 99.9% by weight of zinc, 0.05% by weight of cobalt and 0.05% by weight of molybdenum, has the following composition: Zn ++ 1.91 mol/litre Co ++ 0.10 mol/litre Mo ++ 0.002 mol/litre Mg ++ 0.20 mol/litre
  • the starting materials used to prepare the abovementioned bath were: zinc sulphate heptahydrate 550 grams/litre cobalt sulphate heptahydrate 30 grams/litre (NH 4 ) 6 Mo 7 O 24 .4H 2 O 0.35 gram/litre magnesium sulphate heptahydrate 50 grams/litre
  • the operating conditions were: bath temperature 25°C bath pH 2 cathode current density (zinc anodes) 25 A/dm 2 throughput speed of the wire 18 m/min
  • coatings of similar thickness consisting of a Zn/Fe/Mo or Zn/Ni/Mo ternary alloy, respectively.
  • a galvanic bath capable of depositing on a steel wire a layer of a zinc/cobalt/molybdenum ternary alloy consisting of 95% by weight of zinc, 2% by weight of cobalt and 3% by weight of molybdenum, has the following composition: Zn ++ 1.565 mol/litre Co ++ 0.43 mol/litre Mo ++ 0.0085 mol/litre Mg ++ 0.20 mol/litre
  • the starting materials used to prepare the abovementioned bath were: zinc sulphate heptahydrate 450 grams/litre cobalt sulphate heptahydrate 120 grams/litre (NH 4 ) 6 Mo 7 O 24 .4H 2 O 1.25 grams/litre magnesium sulphate heptahydrate 50 grams/litre
  • the operating conditions were: bath temperature 35°C bath pH 2 cathode current density (zinc anodes) 35 A/dm 2 throughput speed of the wire 25 m/min
  • coatings of similar thickness consisting of a Zn/Fe/Mo or Zn/Ni/Mo ternary alloy, respectively.
  • a galvanic bath capable of depositing on a steel wire a layer of a zinc/cobalt/molybdenum ternary alloy consisting of 99.1% by weight of zinc, 0.5% by weight of cobalt and 0.4% by weight of molybdenum, has the following composition: Zn ++ 1.91 mol/litre Co ++ 0.43 mol/litre Mo ++ 0.004 mol/litre Mg ++ 0.20 mol/litre
  • the starting materials used to prepare the abovementioned bath were: zinc sulphate heptahydrate 550 grams/litre cobalt sulphate heptahydrate 120 grams/litre (NH 4 ) 6 Mo 7 O 24 .4H 2 O 0.75 gram/litre magnesium sulphate heptahydrate 50 grams/litre
  • the operating conditions were: bath temperature 25°C bath pH 2 cathode current density (zinc anodes) 35 A/dm 2 throughput speed of the wire 36 m/min
  • coatings of similar thickness consisting of a Zn/Fe/Mo or Zn/Ni/Mo ternary alloy, respectively.
  • the corrosion resistance was determined by measuring the time required to initiate the formation of rust and of zinc oxide on a steel wire (1.30 mm in diameter) coated according to the invention, immersed in an aqueous 4% NaCI solution at 25°C.
  • the coating had the following composition:
  • Example 4 The process was performed as in Example 4 above, except that the test was carried out on five steel wires (1.30 mm in diameter) coated according to the prior art.
  • the coatings had the following compositions:
  • the adhesion to the vulcanized elastomeric material was measured on test pieces of vulcanized mixture on a steel strand of the invention (made up of 4 wires 0.22 mm in diameter) by the method described in "Kautschk und Gummi Kunststoffe", 5 , 228-232 (1969), which measures the force required to pull a cord out of a cylinder of vulcanized rubber.
  • the "pull-out force" was measured in Newtons using an electronic dynamometer. The values were measured both on freshly prepared vulcanized test pieces and on test pieces after age-hardening for one week at a temperature of 65°C and at 90% relative humidity (R.H.).
  • composition of the mixture which formed the vulcanized rubber was, in parts % by weight, as follows: natural rubber 100 ZnO 8 divalent cobalt 0.2 carbon black 50 silica 10 resorcinol 3 hexamethoxymethylenemelamine 2.4 dicyclohexylbenzothiazolesulphenamide 1.1 sulphur 4 trimercaptotriazine 0.5
  • test pieces of mixture having the abovementioned composition, vulcanized on two steel strands of the prior art (each made up of 4 wires 0.22 mm in diameter) were used.
  • the number of metres of wire produced before the dies needed to be replaced were thus measured.
  • the weight percentage of loss of Zn/Co/Mo alloy deposited was also measured.
  • Example 6 The process was performed in a similar manner to that of Example 6 above, except that two steel wires of the prior art were drawn.
  • Table 6 shows the results obtained. Coating metres of wire produced ⁇ 10 3 loss of coating deposited (%) brass 2000 12 ZnCo 1000 15
  • Cylindrical test samples were prepared by burying steel wire cords (3x4x0.22) coated with a ZnCoMo alloy layer (comprising 0.5% of Co and 0.4% of Mo) having 0.20 micron thick, in a mixture having the composition shown herein below. The mixture was then vulcanized at 151°C for 40 minutes.
  • the burial length of the cords in the test samples was 12 mm.
  • Adhesion was measured in a similar manner to that of Example 5 above, except that the test samples were prepared as described in the - Example 7 above.
  • the pull out force was measured in Newtons with an electronic dynamometer.
  • the coating degree of the cords extracted from each test sample was graded according to a coating index ranking from 1 to 4 depending on the percent of the cord surface which was still well coated by elastomeric material.
  • Test I Initial adhesion values
  • Test II the adhesion values measured after having kept the test samples in a climatic room at 65°C and 90% R.H. for 8 days
  • Table 7 the first number is the adhesion value, as an average on 8 tests, while the index in brackets is the coating degree of the cords. 3x4x0.22 Cord Test I 646 (4) Test II 636 (3.5)

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Claims (30)

  1. Verstärkungsstruktur für aus vulkanisiertem Elastomermaterial hergestellte Erzeugnisse, die eine Vielzahl von Cords umfasst, von denen jeder aus einer Vielzahl oberflächenbehandelter Stahldrähte zusammengesetzt ist, dadurch gekennzeichnet, dass die Drähte mit einer ZnMoX-Legierung beschichtet sind, wobei X ein Metall ist, ausgewählt aus der Gruppe Cobalt, Eisen und Nickel.
  2. Verstärkungsstruktur nach Anspruch 1, dadurch gekennzeichnet, dass die Legierung einen Mo-Gehalt von 0,05 bis 3 Gew.-% aufweist.
  3. Verstärkungsstruktur nach Anspruch 2, dadurch gekennzeichnet, dass die Legierung einen Mo-Gehalt von 0,1 bis 1 Gew.-% aufweist.
  4. Verstärkungsstruktur nach Anspruch 1, dadurch gekennzeichnet, dass die Legierung einen Zn-Gehalt von 95 bis 99,9 Gew.-% aufweist.
  5. Verstärkungsstruktur nach Anspruch 4, dadurch gekennzeichnet, dass die Legierung einen Zn-Gehalt von 98 bis 99,5 Gew.-% aufweist.
  6. Verstärkungsstruktur nach Anspruch 1, dadurch gekennzeichnet, dass die Legierung einen Gehalt des Metalls X von 0,05 bis 2 Gew.-% aufweist.
  7. Verstärkungsstruktur nach Anspruch 6, dadurch gekennzeichnet, dass die Legierung einen Gehalt des Metalls X von 0,1 bis 1 Gew.-% aufweist.
  8. Verstärkungsstruktur nach Anspruch 1, dadurch gekennzeichnet, dass die Legierung durch elektrochemische Abscheidung auf die Oberfläche des Stahldrahts gebildet wird.
  9. Erzeugnis, hergestellt aus vulkanisiertem Elastomermaterial, das einen Stahldraht umfasst, dadurch ge-kennzeichnet, dass der Draht mit einer ZnMoX-Legierung beschichtet ist, wobei X ein Metall ist, ausgewählt aus der Gruppe Cobalt, Eisen und Nickel.
  10. Erzeugnis nach Anspruch 9, dadurch gekennzeichnet, dass die Legierung einen Mo-Gehalt von 0,05 bis 3 Gew.-% aufweist.
  11. Erzeugnis nach Anspruch 10, dadurch gekennzeichnet, dass die Legierung einem Mo-Gehalt von 0,1 bis 1 Gew.-% aufweist.
  12. Erzeugnis nach Anspruch 9, dadurch gekennzeichnet, dass die Legierung einen Zn-Gehalt von 95 bis 99,9 Gew.-% aufweist.
  13. Erzeugnis nach Anspruch 12, dadurch gekennzeichnet, dass die Legierung einen Zn-Gehalt von 98 bis 99,5 Gew.-% aufweist.
  14. Erzeugnis nach Anspruch 9, dadurch gekennzeichnet, dass die Legierung einen Gehalt an Metall X von 0,05 bis 2 Gew.-% aufweist.
  15. Erzeugnis nach Anspruch 14, dadurch gekennzeichnet, dass die Legierung einen Gehalt an Metall X von 0,1 bis 1 Gew.-% aufweist.
  16. Erzeugnis nach Anspruch 9, dadurch gekennzeichnet, dass die Legierung durch elektrochemische Abscheidung auf die Oberfläche des Stahldrahts gebildet wird.
  17. Erzeugnis, das wenigstens einen Metalldraht umfasst, der in eine vulkanisierte Elastomer-Grundmasse eingebettet ist, erhalten aus einem Gemisch, das wenigstens ein vulkanisierbares Elastomer und wenigstens ein Vulkanisationsmittel, das aus Schwefel oder einem Derivat davon besteht, umfasst, dadurch gekennzeichnet, dass der Metalldraht aus einem mit einer ZnMoX-Legierung beschichteten Stahl hergestellt ist, in der X ein Metall ist, ausgewählt aus der Gruppe Cobalt, Eisen und Nickel, und das Gemisch außerdem ein Salz von zweiwertigem Cobalt in einer Menge, die wenigstens 0,2 Gew.-% des zweiwertigen Cobaltmetalls entspricht, bezogen auf das Gewicht des Elastomers, umfasst.
  18. Erzeugnis nach Anspruch 17, dadurch gekennzeichnet, dass die Legierung einen Mo-Gehalt von 0,05 bis 3 Gew.-% aufweist.
  19. Erzeugnis nach Anspruch 18, dadurch gekennzeichnet, dass die Legierung einen Mo-Gehalt von 0,1 bis 1 Gew.-% aufweist.
  20. Erzeugnis nach Anspruch 17, dadurch gekennzeichnet, dass die Legierung einen Zn-Gehalt von 95 bis 99,9 Gew.-% aufweist.
  21. Erzeugnis nach Anspruch 20, dadurch gekennzeichnet, dass die Legierung einen Zn-Gehalt von 98 bis 99,5 Gew.-% aufweist.
  22. Erzeugnis nach Anspruch 17, dadurch gekennzeichnet, dass die Legierung einen Gehalt an Metall X von 0,05 bis 2 Gew.-% aufweist.
  23. Erzeugnis nach Anspruch 22, dadurch gekennzeichnet, dass die Legierung einen Gehalt an Metall X von 0,1 bis 1 Gew.-% aufweist.
  24. Erzeugnis nach Anspruch 17, dadurch gekennzeichnet, dass die Legierung durch elektrochemische Abscheidung auf die Oberfläche des Stahldrahtes gebildet wird.
  25. Erzeugnis nach Anspruch 17, dadurch gekennzeichnet, dass die Menge des Salzes des zweiwertigen Cobalts einer Menge des zweiwertigen Cobaltmetalls von 0,2 bis 1 Gew.-%, bezogen auf das Gewicht des Elastomers, entspricht.
  26. Erzeugnis nach Anspruch 17 oder 25, dadurch gekennzeichnet, dass das Salz des zweiwertigen Cobalts ausgewählt ist aus der Gruppe, die ein Carboxylat der Formel (I) (R-CO-O)2Co worin R eine C6-24-aliphatische oder aromatische Gruppe bedeutet, und einen Co-B-Komplex der Formel (II)
    Figure 00240001
    worin R', R" und R''' gleich oder verschieden sind und eine C6-24-aliphatische oder aromatische Gruppe bedeuten, sowie ein Gemisch davon umfasst.
  27. Erzeugnis nach Anspruch 26, dadurch gekennzeichnet, dass R-CO-O-, R'-CO-O-, R"-CO-O- und R'''-CO-O- ausgewählt sind aus der Gruppe, die n-Heptanoat, 2,2-Dimethylpentanoat, 2-Ethyl-pentanoat, 4,4-Dimethyl-pentanoat, 2-Ethyl-esanoat, n-Octanoat, 2,2-Dimethylesanoat, Neodecanoat und Naphtenat umfasst.
  28. Erzeugnis nach einem der Ansprüche 17 bis 27, dadurch gekennzeichnet, dass das Salz des zweiwertigen Cobalts der Formel (I) Co-Neodecanoat ist.
  29. Erzeugnis nach einem der Ansprüche 17 bis 27, dadurch gekennzeichnet, dass das Salz des zweiwertigen Cobalts der Formel (II) Co-B-2-ethyl-esanoatneodecanoat ist.
  30. Erzeugnis nach einem der Ansprüche 17 bis 29, dadurch gekennzeichnet daß das Erzeugnis ein Reifen, ein Förderband, ein Transmissionsriemen oder ein biegsamer Schlauch ist.
EP99200870A 1998-03-27 1999-03-19 Oberflächenbehandeltes Metallkomponent für die Verstärkung von Strukturen für Produkte aus vulkanisiertem elastomerem Material und daraus hergestellter Gegenstand Expired - Lifetime EP0949356B1 (de)

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EP98830183 1998-03-27
EP98830183 1998-03-27
EP99200870A EP0949356B1 (de) 1998-03-27 1999-03-19 Oberflächenbehandeltes Metallkomponent für die Verstärkung von Strukturen für Produkte aus vulkanisiertem elastomerem Material und daraus hergestellter Gegenstand

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EP0949356A1 EP0949356A1 (de) 1999-10-13
EP0949356B1 true EP0949356B1 (de) 2002-10-23

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EP99200870A Expired - Lifetime EP0949356B1 (de) 1998-03-27 1999-03-19 Oberflächenbehandeltes Metallkomponent für die Verstärkung von Strukturen für Produkte aus vulkanisiertem elastomerem Material und daraus hergestellter Gegenstand

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EP (1) EP0949356B1 (de)
JP (1) JP4351756B2 (de)
KR (1) KR100554047B1 (de)
CN (1) CN1148469C (de)
AT (1) ATE226650T1 (de)
AU (1) AU739167B2 (de)
BR (1) BR9901034B1 (de)
DE (1) DE69903588T2 (de)
ES (1) ES2186298T3 (de)
ID (1) ID23471A (de)
PT (1) PT949356E (de)
TR (1) TR199900710A3 (de)
ZA (1) ZA992283B (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001038426A1 (en) * 1999-11-23 2001-05-31 Pirelli Pneumatici S.P.A. A manufactured article comprising at least one metallic element embedded in a vulcanized elastomeric material
BRPI0418686B1 (pt) 2004-03-31 2013-07-23 método e aparelho para produzir um fio de aço revestido
EP2162299B1 (de) 2007-06-05 2012-08-08 Pirelli Tyre S.P.A. Reifen mit einem Metallkord
JP5625407B2 (ja) * 2010-03-16 2014-11-19 Ｊｆｅスチール株式会社 電気亜鉛めっき鋼板の製造方法
JP5333332B2 (ja) * 2010-04-13 2013-11-06 新日鐵住金株式会社 ゴムとの接着性に優れた極細めっき鋼線
CN110938849A (zh) * 2019-10-29 2020-03-31 湖北第二师范学院 一种锌钼合金镀层钛合金及其制备方法
KR102603735B1 (ko) * 2021-10-18 2023-11-21 넥센타이어 주식회사 타이어 트레드 고무 조성물, 이로부터 제조된 타이어 및 상기 타이어 트레드 고무 조성물의 제조 방법

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4265678A (en) * 1977-12-27 1981-05-05 Tokyo Rope Mfg. Co., Ltd. Metal wire cord
GB1598388A (en) * 1978-05-26 1981-09-16 Bekaert Sa Nv Steel wire reinforcing elements
JPS6134194A (ja) * 1984-07-26 1986-02-18 Hitachi Ltd 複層電気亜鉛合金めつき鋼板およびその製造方法
JPH02310103A (ja) * 1989-05-25 1990-12-25 Bridgestone Corp 重荷重用ラジアルタイヤ
IT1246740B (it) * 1990-12-27 1994-11-26 Pirelli Cavi Spa Articolo comprendente almeno un filo metallico annegato in un materiale elastomerico vulcanizzato.
IT1251401B (it) * 1991-09-09 1995-05-09 Pirelli Filo metallico con doppio strato di rivestimento per il rinforzo di articoli in materiali elastomerici e articoli in materiali elastomerici rinforzati con detto filo.
IT1273334B (it) * 1994-02-24 1997-07-08 Pirelli Filo metallico trattato superficialmente per renderlo adatto all'impiego in elementi compositi in materiale elastomerico e procedimento per la sua realizzazione

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DE69903588T2 (de) 2004-03-18
BR9901034B1 (pt) 2010-12-14
KR100554047B1 (ko) 2006-02-22
TR199900710A2 (xx) 1999-10-21
ES2186298T3 (es) 2003-05-01
KR19990078340A (ko) 1999-10-25
ATE226650T1 (de) 2002-11-15
JP4351756B2 (ja) 2009-10-28
CN1148469C (zh) 2004-05-05
ZA992283B (en) 1999-09-27
AU2131199A (en) 1999-10-07
DE69903588D1 (de) 2002-11-28
AU739167B2 (en) 2001-10-04
TR199900710A3 (tr) 1999-10-21
JP2000054185A (ja) 2000-02-22
ID23471A (id) 2000-04-27
BR9901034A (pt) 2001-11-20
PT949356E (pt) 2003-03-31
CN1236829A (zh) 1999-12-01
EP0949356A1 (de) 1999-10-13

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